| Acute disseminated encephalomyelitis: updates on an inflammatory CNS syndrome D Pohl, G Alper, K Van Haren, AJ Kornberg, CF Lucchinetti, ... Neurology 87 (9_Supplement_2), S38-S45, 2016 | 511 | 2016 |
| A novel outbreak enterovirus D68 strain associated with acute flaccid myelitis cases in the USA (2012–14): a retrospective cohort study AL Greninger, SN Naccache, K Messacar, A Clayton, G Yu, S Somasekar, ... The Lancet Infectious Diseases 15 (6), 671-682, 2015 | 410 | 2015 |
| Clinical approach to the diagnosis of autoimmune encephalitis in the pediatric patient T Cellucci, H Van Mater, F Graus, E Muscal, W Gallentine, ... Neurology: Neuroimmunology & Neuroinflammation 7 (2), e663, 2020 | 230 | 2020 |
| Acute flaccid myelitis: a clinical review of US cases 2012–2015 K Messacar, TL Schreiner, K Van Haren, M Yang, CA Glaser, KL Tyler, ... Annals of neurology 80 (3), 326-338, 2016 | 225 | 2016 |
| Safety and immunologic effects of high-vs low-dose cholecalciferol in multiple sclerosis ES Sotirchos, P Bhargava, C Eckstein, K Van Haren, M Baynes, A Ntranos, ... Neurology 86 (4), 382-390, 2016 | 174 | 2016 |
| Acute flaccid myelitis of unknown etiology in California, 2012-2015 K Van Haren, P Ayscue, E Waubant, A Clayton, H Sheriff, S Yagi, ... Jama 314 (24), 2663-2671, 2015 | 140 | 2015 |
| De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy JR Lee, M Srour, D Kim, FF Hamdan, SH Lim, C Brunel‐Guitton, ... Human mutation 36 (1), 69-78, 2015 | 133 | 2015 |
| Acute flaccid myelitis: cause, diagnosis, and management OC Murphy, K Messacar, L Benson, R Bove, JL Carpenter, T Crawford, ... The Lancet 397 (10271), 334-346, 2021 | 114 | 2021 |
| Acute flaccid paralysis with anterior myelitis—California, June 2012–June 2014 P Ayscue, K Van Haren, H Sheriff, E Waubant, P Waldron, S Yagi, C Yen, ... MMWR Morb Mortal Wkly Rep 63 (40), 903-6, 2014 | 112 | 2014 |
| The unfolded protein response in vanishing white matter disease JP Van Der Voorn, B Van Kollenburg, G Bertrand, K Van Haren, ... Journal of Neuropathology & Experimental Neurology 64 (9), 770-775, 2005 | 110 | 2005 |
| Natural history of vanishing white matter EMC Hamilton, HDW van der Lei, G Vermeulen, JAM Gerver, ... Annals of neurology 84 (2), 274-288, 2018 | 97 | 2018 |
| The life and death of oligodendrocytes in vanishing white matter disease K Van Haren, JP Van Der Voorn, DR Peterson, MS Van Der Knaap, ... Journal of Neuropathology & Experimental Neurology 63 (6), 618-630, 2004 | 91 | 2004 |
| Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function GI Rice, S Park, F Gavazzi, LA Adang, LA Ayuk, L Van Eyck, L Seabra, ... Human mutation 41 (4), 837-849, 2020 | 72 | 2020 |
| Identification of naturally occurring fatty acids of the myelin sheath that resolve neuroinflammation PP Ho, JL Kanter, AM Johnson, HK Srinagesh, EJ Chang, TM Purdy, ... Science translational medicine 4 (137), 137ra73-137ra73, 2012 | 70 | 2012 |
| Safety, tolerability, and efficacy of fluoxetine as an antiviral for acute flaccid myelitis K Messacar, S Sillau, SE Hopkins, C Otten, M Wilson-Murphy, B Wong, ... Neurology 92 (18), e2118-e2126, 2019 | 66 | 2019 |
| Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophies LA Adang, O Sherbini, L Ball, M Bloom, A Darbari, H Amartino, D DiVito, ... Molecular genetics and metabolism 122 (1-2), 18-32, 2017 | 62 | 2017 |
| Disease specific therapies in leukodystrophies and leukoencephalopathies G Helman, K Van Haren, JL Bonkowsky, G Bernard, A Pizzino, ... Molecular genetics and metabolism 114 (4), 527-536, 2015 | 62 | 2015 |
| Clinical subpopulations in a sample of North American children diagnosed with acute flaccid myelitis, 2012-2016 MJ Elrick, E Gordon-Lipkin, TO Crawford, K Van Haren, K Messacar, ... JAMA pediatrics 173 (2), 134-139, 2019 | 60 | 2019 |
| Serum autoantibodies to myelin peptides distinguish acute disseminated encephalomyelitis from relapsing–remitting multiple sclerosis K Van Haren, BH Tomooka, BA Kidd, B Banwell, A Bar-Or, T Chitnis, ... Multiple Sclerosis Journal 19 (13), 1726-1733, 2013 | 55 | 2013 |
| MRI surveillance of boys with X‐linked adrenoleukodystrophy identified by newborn screening: meta‐analysis and consensus guidelines EJ Mallack, BR Turk, H Yan, C Price, M Demetres, AB Moser, C Becker, ... Journal of inherited metabolic disease 44 (3), 728-739, 2021 | 52 | 2021 |
lawrence steinmanstanford universityVerified email at stanford.edu
